Chang S M, Barker F G, Huhn S L, Nicholas M K, Page M, Rabbitt J, Prados M D
Brain Tumor Research Center, Department of Neurological Surgery, University of California, San Francisco 94117, USA.
J Neurooncol. 1998 Apr;37(2):169-76. doi: 10.1023/a:1005826323652.
Chemotherapeutic regimens in present use for recurrent glioma have substantial toxicity. Activity against recurrent gliomas has been reported for both tamoxifen and interferon alpha, agents that have more acceptable toxicity profiles and that can be administered in an outpatient setting. We tested the efficacy and toxicity of the combination of high-dose tamoxifen and interferon alpha in adults with recurrent glioma in a phase II trial. Eligible patients had radiographically measurable recurrent gliomas of any grade after initial radiation therapy. Interferon-alpha [6 x 10(6) U subcutaneously three times per week] and tamoxifen (240 mg/m2/day orally) were administered continuously. Treatment response was assessed at 6 week intervals using clinical and radiographic criteria. Eighteen patients (11 males and 7 females) were enrolled. Median age was 41 years (range 23-61 years). All patients had gliomas that progressed after radiation therapy and nitrosourea chemotherapy. The histologic diagnosis of the original tumor was glioblastoma multiforme in 8 patients, anaplastic astrocytoma in 5 patients, astrocytoma in 4 patients and mixed malignant glioma in 1 patient. Reversible moderate to severe neurological toxicity manifested by dizziness and unsteady gait was seen at tamoxifen doses of 240 mg/m2/day. Although the initial tamoxifen dose was reduced to 120 mg/m2/day, moderate neurotoxicity was noted at this dose as well and the trial was closed early. The combination of oral tamoxifen (120 to 240 mg/m2/day) and subcutaneous interferon-alpha [6 x 10(6) U three times per week] was associated with significant neurotoxicity in this group of recurrent glioma patients, resulting in early study closure. Of 16 evaluable patients, 12 had progressive disease after one cycle of treatment, 3 had stable disease, and there was one minor response. Gradual dose escalation may be required if similar patients are to be treated with high dose tamoxifen in conjunction with interferon.
目前用于复发性神经胶质瘤的化疗方案具有很大的毒性。他莫昔芬和α干扰素对复发性神经胶质瘤均有活性,这两种药物的毒性特征更易接受,且可在门诊给药。我们在一项II期试验中测试了高剂量他莫昔芬和α干扰素联合用药对成年复发性神经胶质瘤患者的疗效和毒性。符合条件的患者在初次放疗后患有影像学上可测量的任何级别的复发性神经胶质瘤。持续给予α干扰素[6×10(6)单位,皮下注射,每周3次]和他莫昔芬(240mg/m2/天,口服)。每隔6周根据临床和影像学标准评估治疗反应。18例患者(11例男性和7例女性)入组。中位年龄为41岁(范围23 - 61岁)。所有患者的神经胶质瘤在放疗和亚硝基脲化疗后均进展。原发肿瘤的组织学诊断为多形性胶质母细胞瘤8例,间变性星形细胞瘤5例,星形细胞瘤4例,混合性恶性神经胶质瘤1例。当他莫昔芬剂量为240mg/m2/天时,出现了以头晕和步态不稳为表现的可逆性中度至重度神经毒性。尽管最初将他莫昔芬剂量降至120mg/m2/天,但在此剂量下仍观察到中度神经毒性,试验提前终止。口服他莫昔芬(120至240mg/m2/天)和皮下注射α干扰素[6×10(6)单位,每周3次]的联合用药在这组复发性神经胶质瘤患者中具有显著的神经毒性,导致研究提前结束。在16例可评估患者中,12例在一个治疗周期后病情进展,3例病情稳定,1例有轻微反应。如果要用高剂量他莫昔芬联合干扰素治疗类似患者,可能需要逐步增加剂量。